Immunostimulating Interstitial Laser Thermotherapy in Malignant Melanoma
Primary Purpose
Melanoma, Malignant Melanoma
Status
Terminated
Phase
Not Applicable
Locations
Sweden
Study Type
Interventional
Intervention
Immunostimulating Interstitial Laser Thermotherapy
Sponsored by
About this trial
This is an interventional treatment trial for Melanoma focused on measuring Hyperthermia, Induced, Laser Coagulation, Laser Therapy
Eligibility Criteria
Inclusion Criteria:
- >18 years of age
- histologically confirmed malignant melanoma
- advanced melanoma disease (Stage III inoperable or Stage IV) that has progressed on standard first line treatment such as kinase inhibitor(s) and/or immunoregulatory monoclonal antibodies. Previously untreated patients with a dominant tumour lesion deemed suitable for local and highly tumour-destructive ablation may also be included
- time interval between previous systemic treatment and imILT of at least one month
- at least one lesion located in such a way (typically subcutaneously) that it can be treated without risk of skin necrosis or serious damage to other adjacent vital and healthy tissue
- verbal and written informed consent to participate
- adequate haematologic, renal and hepatic functions
- have an ECOG performance status ≤ 2 (Karnofsky ≥ 60%)
Exclusion Criteria:
- known HIV infection
- autoimmune disease which is judged to reduce an anti-tumour immune response
- systemic corticosteroid medication
- bleeding diathesis
- pregnancy or breast-feeding
Sites / Locations
- Karolinska University Hospital Solna
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
imILT
Arm Description
Immunostimulating Interstitial Laser Thermotherapy (imILT)
Outcomes
Primary Outcome Measures
Safety (adverse events)
Evaluation of adverse events.
Usability of the device as evaluated by treatment logs
Evaluation of the laser system by analysis of treatment logs of the device.
Usability of the device as evaluated by user questionnaire
Evaluation of the laser system by analysis of user questionnaire.
Secondary Outcome Measures
Treatment effect (Measurement of tumor burden by irRC criteria)
Measurement of tumor burden by irRC criteria.
Inflammatory response in tumor and circulation measured by quantification of inflammatory cell populations
Quantification of cellular infiltrate and activation markers by immunohistochemistry and flow cytometry.
Full Information
NCT ID
NCT02650492
First Posted
November 27, 2015
Last Updated
July 2, 2021
Sponsor
Clinical Laserthermia Systems AB
1. Study Identification
Unique Protocol Identification Number
NCT02650492
Brief Title
Immunostimulating Interstitial Laser Thermotherapy in Malignant Melanoma
Official Title
Exploratory Study on Immunostimulating Interstitial Laser Thermotherapy in Malignant Melanoma
Study Type
Interventional
2. Study Status
Record Verification Date
July 2021
Overall Recruitment Status
Terminated
Why Stopped
Study was stopped in agreement with investigator due to slow patient recruitment.
Study Start Date
October 2015 (Actual)
Primary Completion Date
November 1, 2016 (Actual)
Study Completion Date
May 1, 2019 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Clinical Laserthermia Systems AB
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Thermotherapy is a technology aiming at destroying tissue, for example tumor tissue. Immunostimulating Interstitial Laser Thermotherpy (imILT) is a specific form of thermotherapy, which, in addition to destroying tumor tissue, has been optimized to cause a tumor specific immunologic response. In laboratory animals the imILT method has also been shown to induce a so called abscopal effect. This means that when one tumor is treated with imILT other, untreated, tumors also decrease in size. The immunologic response has previously been characterized in breast cancer patients after receiving imILT treatment , and presumed abscopal effects induced by imILT have also been described in a malignant melanoma patient.
The purpose of this trial is to investigate the functionality and safety of the imILT treatment method in patients diagnosed with malignant melanoma. The inflammatory process, following on the treatment, will also be described in order to provide a more in depth knowledge of the treatment for this indication. The purpose is also to evaluate efficiency when it comes to local tumor destruction as well as understanding of the subsequent immunological effects. Since immunologically based treatment of malignant melanoma is under intense review with so called "immune checkpoint inhibitors" this trial will also provide valuable information on how imILT, in the future, could be combined with these new and, for some patients, very effective treatment regimens.
The treatment method has successfully been used for treatment of patients with breast cancer and malignant melanoma . Treatment of breast cancer patients caused an increase of cytotoxic T lymphocytes in the treated tumor, as well as activated dendritic cells at the tumor border. Regulatory T lymphocytes decreased in the regional lymph nodes.
This trial is explorative, prospective, open and non-randomized. Five malignant melanoma patients stage III - IV will be treated in this trial, which is estimated to be carried out during a time period of 12 months.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Melanoma, Malignant Melanoma
Keywords
Hyperthermia, Induced, Laser Coagulation, Laser Therapy
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
2 (Actual)
8. Arms, Groups, and Interventions
Arm Title
imILT
Arm Type
Experimental
Arm Description
Immunostimulating Interstitial Laser Thermotherapy (imILT)
Intervention Type
Device
Intervention Name(s)
Immunostimulating Interstitial Laser Thermotherapy
Intervention Description
Immunostimulating Interstitial Laser Thermotherpy (imILT) is a specific form of thermotherapy, which, in addition to destroying tumor tissue, has been optimized to cause a tumor specific immunologic response.
Primary Outcome Measure Information:
Title
Safety (adverse events)
Description
Evaluation of adverse events.
Time Frame
18 months
Title
Usability of the device as evaluated by treatment logs
Description
Evaluation of the laser system by analysis of treatment logs of the device.
Time Frame
18 months
Title
Usability of the device as evaluated by user questionnaire
Description
Evaluation of the laser system by analysis of user questionnaire.
Time Frame
18 months
Secondary Outcome Measure Information:
Title
Treatment effect (Measurement of tumor burden by irRC criteria)
Description
Measurement of tumor burden by irRC criteria.
Time Frame
18 months
Title
Inflammatory response in tumor and circulation measured by quantification of inflammatory cell populations
Description
Quantification of cellular infiltrate and activation markers by immunohistochemistry and flow cytometry.
Time Frame
18 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
>18 years of age
histologically confirmed malignant melanoma
advanced melanoma disease (Stage III inoperable or Stage IV) that has progressed on standard first line treatment such as kinase inhibitor(s) and/or immunoregulatory monoclonal antibodies. Previously untreated patients with a dominant tumour lesion deemed suitable for local and highly tumour-destructive ablation may also be included
time interval between previous systemic treatment and imILT of at least one month
at least one lesion located in such a way (typically subcutaneously) that it can be treated without risk of skin necrosis or serious damage to other adjacent vital and healthy tissue
verbal and written informed consent to participate
adequate haematologic, renal and hepatic functions
have an ECOG performance status ≤ 2 (Karnofsky ≥ 60%)
Exclusion Criteria:
known HIV infection
autoimmune disease which is judged to reduce an anti-tumour immune response
systemic corticosteroid medication
bleeding diathesis
pregnancy or breast-feeding
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Johan Hansson, MD PhD
Organizational Affiliation
Karolinska Institutet
Official's Role
Principal Investigator
Facility Information:
Facility Name
Karolinska University Hospital Solna
City
Stockholm
ZIP/Postal Code
17176
Country
Sweden
12. IPD Sharing Statement
Learn more about this trial
Immunostimulating Interstitial Laser Thermotherapy in Malignant Melanoma
We'll reach out to this number within 24 hrs